ClinVar Miner

List of variants reported as uncertain significance for cirrhosis, familial

Included ClinVar conditions (2):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000224.3(KRT18):c.206G>C (p.Gly69Ala)	rs532875586	0.00020
NM_000224.3(KRT18):c.541G>A (p.Asp181Asn)	rs1942470902
NM_000224.3(KRT18):c.599A>G (p.Glu200Gly)

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